Efficacy, Safety, and Tolerability of Eluxadoline in the Treatment of Participants With Diarrhea-Predominant Irritable Bowel Syndrome (IBS-d)

Last updated: July 27, 2018
Sponsor: Furiex Pharmaceuticals, Inc
Overall Status: Completed

Phase

3

Condition

Gastrointestinal Diseases And Disorders

Bowel Dysfunction

Colic

Treatment

N/A

Clinical Study ID

NCT01553747
27018966IBS3002
2012-001601-24
  • Ages 18-80
  • All Genders

Study Summary

The purpose of this study is to determine the efficacy, safety, and tolerability of different doses of eluxadoline (JNJ-27018966) compared with placebo in the treatment of participants with diarrhea-predominant irritable bowel syndrome.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Participant is 18 to 80 years old

  2. Participant has a diagnosis of irritable bowel syndrome (IBS) with a subtype ofdiarrhea defined by the Rome III criteria.

  3. Participant has had a colonoscopy performed:

  • Within 10 years prior to Prescreening if participant is at least 50 years of age (sigmoidoscopy, double contrast barium enema, or computed tomography (CT) colonographywithin the past 5 years is acceptable)

  • Since the onset (if applicable) of any of the following alarm features forparticipants of any age

  • Participant has documented weight loss within the past 6 months

  • Participant has nocturnal symptoms

  • Participant has a familial history of first-degree relatives with colon cancer

  • Participant has blood mixed with their stool (excluding blood from hemorrhoids).

  1. Female participants must be:
  • Postmenopausal, defined as 52 years or older and amenorrheic for at least 2 years atPrescreening,

  • Surgically sterile (have had a hysterectomy or bilateral oophorectomy, tubal ligation,or otherwise be incapable of pregnancy),

  • Abstinent, or

  • If sexually active, be practicing an effective method of birth control.

Exclusion

Exclusion Criteria:

  1. Participant has a diagnosis of IBS with a subtype of constipation, mixed IBS, orunsubtyped IBS by the Rome III criteria.

  2. Participant has a history of inflammatory or immune-mediated gastrointestinal (GI)disorders including inflammatory bowel disease (ie, Crohn's disease, ulcerativecolitis) and celiac disease.

  3. Participant has a history of diverticulitis within 3 months prior to Prescreening.

  4. Participant has a history of intestinal obstruction, stricture, toxic megacolon, GIperforation, fecal impaction, gastric banding, bariatric surgery, adhesions, ischemiccolitis, or impaired intestinal circulation (eg, aortoiliac disease).

  5. Participant has any of the following surgical history:

  • Cholecystectomy with any history of post cholecystectomy biliary tract pain

  • Any abdominal surgery within the 3 months prior to Prescreening

  • Participant has a history of major gastric, hepatic, pancreatic, or intestinalsurgery (appendectomy, hemorrhoidectomy, or polypectomy greater than 3 monthspost surgery are allowed) Other protocol-specific eligibility criteria may apply.

Study Design

Total Participants: 1146
Study Start date:
May 29, 2012
Estimated Completion Date:
January 09, 2014

Connect with a study center

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    Kelowna, British Columbia V1Y 3G8
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    Sarnia, Ontario N7T 4X3
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    Sudbury, Ontario P3E 1H5
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    Vaughan, Ontario L4L 4Y7
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    Warwick, Rhode Island 02888
    United States

    Site Not Available

  • Furiex Research Site

    Anderson, South Carolina 29621
    United States

    Site Not Available

  • Furiex Research Site

    Columbia, South Carolina 29204
    United States

    Site Not Available

  • Furiex Research Site

    Easley, South Carolina 29640
    United States

    Site Not Available

  • Furiex Research Site

    Greenville, South Carolina 29615
    United States

    Site Not Available

  • Furiex Research Site

    Mount Pleasant, South Carolina 29464
    United States

    Site Not Available

  • Furiex Research Site

    Mt. Pleasant, South Carolina 29464
    United States

    Site Not Available

  • Furiex Research Site

    North Myrtle Beach, South Carolina 29582
    United States

    Site Not Available

  • Furiex Research Site

    Orangeburg, South Carolina 29118
    United States

    Site Not Available

  • Furiex Research Site

    Rapid City, South Dakota 57702
    United States

    Site Not Available

  • Furiex Research Site

    Athens, Tennessee 37303
    United States

    Site Not Available

  • Furiex Research Site

    Chattanooga, Tennessee 37404
    United States

    Site Not Available

  • Furiex Research Site

    Jackson, Tennessee 38305
    United States

    Site Not Available

  • Furiex Research Site

    Knoxville, Tennessee 37919
    United States

    Site Not Available

  • Furiex Research Site

    Smyrna, Tennessee 37167
    United States

    Site Not Available

  • Furiex Research Site

    Austin, Texas 78745
    United States

    Site Not Available

  • Furiex Research Site

    Beaumont, Texas 77701
    United States

    Site Not Available

  • Furiex Research Site

    Bedford, Texas 76021
    United States

    Site Not Available

  • Furiex Research Site

    Bellaire, Texas 77401
    United States

    Site Not Available

  • Furiex Research Site

    Corsicana, Texas 75110
    United States

    Site Not Available

  • Furiex Research Site

    Dallas, Texas 75218
    United States

    Site Not Available

  • Furiex Research Site

    Fort Worth, Texas 76133
    United States

    Site Not Available

  • Furiex Research Site

    Frisco, Texas 75035
    United States

    Site Not Available

  • Furiex Research Site

    Grapevine, Texas 76051
    United States

    Site Not Available

  • Furiex Research Site

    Houston, Texas 77008
    United States

    Site Not Available

  • Furiex Research Site

    Humble, Texas 77338
    United States

    Site Not Available

  • Furiex Research Site

    Hurst, Texas 76054
    United States

    Site Not Available

  • Furiex Research Site

    Lake Jackson, Texas 77566
    United States

    Site Not Available

  • Furiex Research Site

    San Antonio, Texas 78215
    United States

    Site Not Available

  • Furiex Research Site

    Spring, Texas 77386
    United States

    Site Not Available

  • Furiex Research Site

    Tyler, Texas 75708
    United States

    Site Not Available

  • Furiex Research Site

    Uvalde, Texas 78801
    United States

    Site Not Available

  • Furiex Research Site

    Bountiful, Utah 84010
    United States

    Site Not Available

  • Furiex Research Site

    Clinton, Utah 84015
    United States

    Site Not Available

  • Furiex Research Site

    Salt Lake City, Utah 84124
    United States

    Site Not Available

  • Furiex Research Site

    West Valley City, Utah 84120
    United States

    Site Not Available

  • Furiex Research Site

    Burlington, Vermont 05401
    United States

    Site Not Available

  • Furiex Research Site

    Alexandria, Virginia 22304
    United States

    Site Not Available

  • Furiex Research Site

    Christiansburg, Virginia 24073
    United States

    Site Not Available

  • Furiex Research Site

    Midlothian, Virginia 23114
    United States

    Site Not Available

  • Furiex Research Site

    Newport News, Virginia 23601
    United States

    Site Not Available

  • Furiex Research Site

    Norfolk, Virginia 23502
    United States

    Site Not Available

  • Furiex Research Site

    Richmond, Virginia 23233
    United States

    Site Not Available

  • Furiex Research Site

    Virginia Beach, Virginia 23451
    United States

    Site Not Available

  • Furiex Research Site

    Tacoma, Washington 98405
    United States

    Site Not Available

  • Furiex Research Site

    Walla Walla, Washington 99362
    United States

    Site Not Available

  • Furiex Research Site

    Charleston, West Virginia 25304
    United States

    Site Not Available

  • Furiex Research Site

    Marshfield, Wisconsin 54449
    United States

    Site Not Available

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